TY - JOUR
T1 - Developing covid-19 vaccines at pandemic speed
AU - Lurie, Nicole
AU - Saville, Melanie
AU - Hatchett, Richard
AU - Halton, Jane
N1 - Funding Information:
Our organization, the Coalition for Epidemic Preparedness Inno vation (CEPI), an international nongovernmental organization funded by the Wellcome Trust, the Bill and Melinda Gates Foun dation, the European Commission, and eight countries (Australia, Belgium, Canada, Ethiopia, Ger many, Japan, Norway, and the United Kingdom), is supporting development of vaccines against five epidemic pathogens on the World Health Organization (WHO) priority list. We aim to develop reserves of investigational vaccines for each pathogen after such vac cines have completed phase 2a trials, expecting that they will undergo clinical trials during fu ture outbreaks. CEPI also sup ports development of platform technologies to prepare for “Dis ease X” — a newly emerging epi demic disease, such as Covid-19. An ideal platform would support development from viral sequenc ing to clinical trials in less than 16 weeks, demonstrate elicitation of consistent immune responses across pathogens, and be suitable for large-scale manufacturing us ing a pathogen-agnostic platform.
PY - 2020/5/21
Y1 - 2020/5/21
N2 - The need to rapidly develop a vaccine against SARS-CoV-2 comes at a time of explosion in basic scientific understanding, including in areas such as genomics and structural biology, that is supporting a new era in vaccine development. Over the past decade, the scientific community and the vaccine industry have been asked to respond urgently to epidemics of H1N1 influenza, Ebola, Zika, and now SARS-CoV-2. An H1N1 influenza vaccine was developed relatively rapidly, largely because influenza-vaccine technology was well developed and key regulators had previously decided that vaccines made using egg- and cell-based platforms could be licensed under the rules used for a strain change. Although a monovalent H1N1 vaccine was not available before the pandemic peaked in the Northern Hemisphere, it was available soon afterward as a stand-alone vaccine and was ultimately incorporated into commercially available seasonal influenza vaccines.
AB - The need to rapidly develop a vaccine against SARS-CoV-2 comes at a time of explosion in basic scientific understanding, including in areas such as genomics and structural biology, that is supporting a new era in vaccine development. Over the past decade, the scientific community and the vaccine industry have been asked to respond urgently to epidemics of H1N1 influenza, Ebola, Zika, and now SARS-CoV-2. An H1N1 influenza vaccine was developed relatively rapidly, largely because influenza-vaccine technology was well developed and key regulators had previously decided that vaccines made using egg- and cell-based platforms could be licensed under the rules used for a strain change. Although a monovalent H1N1 vaccine was not available before the pandemic peaked in the Northern Hemisphere, it was available soon afterward as a stand-alone vaccine and was ultimately incorporated into commercially available seasonal influenza vaccines.
UR - http://www.scopus.com/inward/record.url?scp=85083287982&partnerID=8YFLogxK
U2 - 10.1056/NEJMp2005630
DO - 10.1056/NEJMp2005630
M3 - Review article
C2 - 32227757
AN - SCOPUS:85083287982
SN - 0028-4793
VL - 382
SP - 1969
EP - 1973
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 21
ER -